Seven-membered intramolecular

The synthesis of five-, six-, and seven-membered cyclic esters or timides uses intramolecular condensations under the same reaction condifions as described for intermolecular reactions. Yields are generally excellent. An example from the colchicine synthesis of E.E. van Ta-melen (1961) is given below. The synthesis of macrocyclic lactones (macrolides) and lactams (n > 8), however, which are of considerable biochemical and pharmacological interest, poses additional problems because of competing intermolecular polymerization reactions (see p. 246ff.). Inconveniently high dilution, which would be necessary to circumvent this side-... 

Carbonylation of halides in the presence of primary and secondary amines at I atm affords amides[351j. The intramolecular carbonylation of an aryl bromide which has amino group affords a lactam and has been used for the synthesis of the isoquinoline alkaloid 498(352], The naturally occurring seven-membered lactam 499 (tomaymycin, neothramycin) is prepared by this method(353]. The a-methylene-d-lactam 500 is formed by the intramolecular carbonylation of 2-bromo-3-alkylamino-l-propene(354]. 

Dimethyl iodo(4-pentenyl)malonate (926) undergoes a Pd-catalyzed intramolecular radical-type reaction to form the alkyl iodides 927 and 928. rather than a Heck-type reaction product(775]. The same products are also obtained by a radical reaction promoted by tin hydride(776]. Although yield was low, a similar cyclization of the n-chloro ester 929 to form the seven-membered ring 930 was ob,served(777(. 

Dieckmann cyclization (Section 21.2) An intramolecular analog of the Claisen condensation. Cyclic p-keto esters in which the ring is five- to seven-membered may be formed by using this reaction. 

The intramolecular variant of the Friedel-Crafts alkylation is also synthetically useful, especially for the closure of six-membered rings, e.g. the synthesis of tetraline 8 but five- and seven-membered ring products are also accessible ... 

Alkyl aryl ethers and enol ethers are also accessible by the Mitsunobu method. Cyclic ethers can be obtained by an intramolecular variant, which is especially suitable for the synthesis of three- to seven-membered rings ... 

Many examples of retention of activity in the face of replacement of benzene by thiophene have been noted so far. Application of this stratagem to a clozapine-like antipsychotic constitutes yet another example where activity is retained. The seven-membered ring of the compound in question is established by intramolecular amide formation on intermediate 102. Treatment of amide 103 with N-methylpiperazine in the presence of titanium tetrachloride affords flumezapine (104) [20]. 

RCM was also used in Yamamoto s total synthesis of the marine neurotoxin gambierol (81) [62], to close the central seven-membered E ring, thereby completing the octacyclic polyether core 80 (Scheme 15). Following previously developed methodology [63], metathesis precursor 79 was produced as the major epimer, by boron trifluoride etherate-mediated intramolecular allylation of a-chloroacetoxy ether 78. Subsequent treatment of 79 with catalyst C produced the octacyclic ether 80 in 88% yield. 

The steric and configurational factors discussed above would suggest that five-membered rings should form somewhat more readily than rings of six or seven members, but they offer no explanation for the total exclusion of intermolecular condensation, nor do they explain the much greater rate of intramolecular reaction of five-membered units as compared with the rates of intermolecular reaction of larger units. A possible partial explanation for these peculiarities of five-membered... 

Besides this unique above-described process, there a numerous examples of inter- and intramolecular domino Michael/aldol processes in which the sequence is initiated by the addition of a metalorganic compound to an enone moiety. The Kamimura group [30] synthesized several five- to seven-membered thio- and hy-... 

Chen KY, Cheng YM, Lai CH et al (2007) Ortho green fluorescence protein synthetic chromophore Excited-state intramolecular proton transfer via a seven-membered-ring hydrogen-bonding system. J Am Chem Soc 129 4534 -535... 

Amides and sulfonamides undergo intramolecular chemistry to form aryl amides and aryl sulfonamides (Equations (17)—(19)) in the presence of palladium catalysts ligated by arylphos-phines.35,89 Initially, complexes of P(furyl)3 and P(o-tol)3 were most effective catalysts, but complexes of Hayashi s MOP and van Leeuwen s DPEphos and xantphos have lately been shown to be more active.90 In the presence of catalysts containing one of these ligand systems, five-, six-, and seven-membered rings were formed from halogenated benzamides or from substrates containing an acetamide, an A-carbobenzyloxy, or a t-butylcarbamate substituent tethered to the aryl halide (Equations (18) and (19)) ... 

A synthetically useful application of an intramolecular microwave-assisted Heck reaction has been described by Gracias and coworkers (Scheme 6.9) [28], In their approach toward the synthesis of N-containing seven-membered heterocycles, the... 

The ene reaction (equation 42) is the indirect substituting addition of an unsaturated compound X = Y to an olefin possessing an allylic hydrogen atom, which is transferred in the process44,45. The intramolecular version of the reaction (equation 43) has been applied to the formation of five-, six- and seven-membered rings46. 

Stereospecific contraction of the seven-membered nucleus was observed on treatment of the dimesylated thiepanetetrol derivatives 67 (obtained in turn from d-sorbitol) with sodium azide to give a 5 1 mixture of the bis(azido)tetrahydrothiophenes 68 and 69. Intramolecular nucleophilic displacement of either mesylate group initiates this ring contraction <00TA1389>. 

Synthesis ofSeven-membered Cyclic Nitronates Cyclic nitronates containing more than four carbon atoms in the ring remain virtually unknown. Convenient procedures for the synthesis of these compounds are lacking. In particular, intramolecular alkylation of 5-bromo-l-nitropentane affords nitrocy-clopentane rather than the corresponding seven-membered cyclic nitronate (169) (Scheme 3.48). 

However, intramolecular O-alkylation can be performed under particular conditions leading to of annelation of a seven-membered heterocycle. Japanese researchers (170) prepared the corresponding seven-membered cyclic nitronates (50a-c) in good yields by the reaction of triethylamine with brominated aryl ketones (49a-c) containing the nitromethyl group in the ortho position. 

In order to gain more insight into this proposed mechanism, Montgomery and co-workers tried to isolate the intermediate metallacycle. This effort has also led to the development of a new [2 + 2 + 2]-reaction.226 It has been found that the presence of bipyridine (bpy) or tetramethylethylenediamine (TMEDA) makes the isolation of the desired metallacycles possible, and these metallacycles are characterized by X-ray analysis (Scheme 56).227 Besides important mechanistic implications for enyne isomerizations or intramolecular [4 + 2]-cycloadditions,228 the TMEDA-stabilized seven-membered nickel enolates 224 have been further trapped in aldol reactions, opening an access to complex polycyclic compounds and notably triquinanes. Thus, up to three rings can be generated in the intramolecular version of the reaction, for example, spirocycle 223 was obtained in 49% yield as a single diastereomer from dialdehyde 222 (Scheme 56).229... 

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